发生于20世纪80年代的Bjork-Shiley心脏瓣膜事件是美国医疗器械风险管理方面的典型案例之一,该事件最终导致1990年《安全医疗器械法令》(SafeMedicalDevicesAct,SMDA)的发布。本文试图通过对该事件处理过程进行梳理和归纳,以期展现事件发生背景、可能的原因以及带来的影响及后果,由此提出事件处理过程带给我们的启示。
<<Bjork-Shiley heart valve event,happened in the 1980s,was one of the most typical cases in the medical device risk management,which led to the issue of Safe Medical Devices Act(SMDA). In order to reveal the background,potential reasons and the following influence,the handling process of Bjork-Shiley heart valve event was reviewed in this article,in order to provide some suggestions in the medical device risk management.
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